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      Prospective, comprehensive, and effective viral monitoring in Cuban children undergoing solid organ transplantation

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          Abstract

          Purpose

          In Cuba, viral monitoring in the post-transplant period was not routinely performed. The aim of this research is to identify the most frequent viruses that affect transplanted Cuban children, by implementing a viral follow-up during the post-transplant period.

          Methods

          The study population included all Cuban pediatric patients who underwent solid organ transplantation (SOT) between November 2009 and December 2012. A total of 34 transplanted pediatric patients of kidney (n = 11) and liver (n = 23) were prospectively monitored during a 34-week period for viral DNAemia and DNAuria by simultaneous detection of cytomegalovirus (CMV), Epstein-Barr virus, herpes simplex virus type 1 and 2, varicella zoster virus, human herpesvirus 6, human adenovirus, and polyomaviruses (BKV and JCV) using quantitative real-time polymerase chain reaction (qRT-PCR).

          Results

          Viral genome of at least one virus was detected in 21 of 34 recipients, 18 patients excreted virus in urine while 12 presented DNAemia. CMV (41.2%) and BKV (35.3%) were the most frequent viruses detected during the follow-up. CMV was the virus mainly associated with clinical symptoms and DNAemia. Its excretion in urine (with cut off value of 219 copies/mL) was associated with detection in plasma (p < 0.001); furthermore, CMV viruria was predictive of CMV viremia (OR:8.4, CI:2.4-29.1, p = 0.001). There was no association between high viral load and clinical complications, due to the prompt initiation of preemptive ganciclovir. Conclusion: This comprehensive viral monitoring program effectively prevents the development of critical viral disease, thus urge the implementation of qRT-PCR as routine for viral monitoring of transplanted Cuban organ recipients.

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          Most cited references40

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          Adenovirus.

          Adenoviruses (AdV) are DNA viruses that typically cause mild infections involving the upper or lower respiratory tract, gastrointestinal (GI) tract, or conjunctiva. Rare manifestations of AdV infections include hemorrhagic cystitis, hepatitis, hemorrhagic colitis, pancreatitis, nephritis, or encephalitis. Adenovirus infections are more common in young children, owing to lack of humoral immunity. Epidemics of AdV infections may occur in healthy children or adults in closed or crowded settings (particularly military recruits). The disease is more severe, and dissemination is more likely in patients with impaired immunity (eg, organ transplant recipients, human immunodeficiency virus infection, congenital immunodeficiency syndromes). Fatality rates for untreated severe AdV pneumonia or disseminated disease may exceed 50%. More than 50 serotypes of AdV have been identified. Different serotypes display different tissue trophisms and correlate with clinical manifestations of infection. The predominant serotypes differ among countries or regions and change over time. Transmission of novel strains between countries or across continents and replacement of dominant serotypes by new strains may occur. Treatment of AdV infections is controversial because prospective, randomized therapeutic trials have not been done. Cidofovir is considered the drug of choice for severe AdV infections, but not all patients require treatment. Vaccines have been shown to be highly efficacious in reducing the risk of respiratory AdV infection but are currently not available. © Thieme Medical Publishers.
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            American Society of Transplantation recommendations for screening, monitoring and reporting of infectious complications in immunosuppression trials in recipients of organ transplantation.

            In recent years, major progress has been made in the development, investigation and clinical application of novel immunosuppressive drug therapies to prevent acute rejection. Critical to the ultimate clinical application of new drug therapies is the ongoing performance of large multi-center clinical trials. However, there has been a paucity of infectious disease monitoring built into these protocols. Given that infectious complications are a major source of morbidity and mortality in transplant recipients, the assessment of the magnitude of risk of infection associated with a given immunosuppressive strategy may be as important as the assessment of rejection. For the above reasons, screening, monitoring and reporting recommendations for common transplant-associated infections were developed for use in clinical trials evaluating immunosuppressive strategies. These recommendations have two major goals: (i) to provide clinically relevant definitions for tracking infectious complications occurring in participants in immunosuppressive trials and (ii) where appropriate, to recommend specific laboratory monitoring and surveillance methods.
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              Evaluation of patients with advanced cancer using the Karnofsky performance status.

              The Karnofsky Performance Status Scale (KPS) was designed to measure the level of patient activity and medical care requirements. It is a general measure of patient independence and has been widely used as a general assessment of patient with cancer. Although there is a long history of use of the KPS for judging cancer patients, its reliability and validity have been assumed without formal investigation. The interrater reliability of the KPS was investigated in two ways, both of which gave evidence of moderately high reliability. The patients evaluated in their home were usually assigned a lower KPS score compared with a similar evaluation at the same time done in the outpatient clinic. Costruct validity of the KPS was demonstrated by strong correlation with several variables relating to physical function. On-study KPS score accurately predicted early death, but high initial KPS scores did not necessarily predict long survival. Patient deterioration with subsequent death within a few months could be predicted to a limited extent by a rapidly dropping KPS. These results suggest that the KPS has considerable validity as a global indicator of the functional status of patients with cancer and might be helpful for following other patients with chronic disease.
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                Author and article information

                Contributors
                vkouri@ipk.sld.cu
                consuelo@ipk.sld.cu
                arielmr@cecmed.sld.cu
                Lizet@ipk.sld.cu
                alinaa@ipk.sld.cu
                grehete@ipk.sld.cu
                vkouri@infomed.sld.cu
                nivette@infomed.sld.cu
                florin@infomed.sld.cu
                lourdesm.perez@infomed.sld.cu
                dipatri@infomed.sld.cu
                yardelis.perez@infomed.sld.cu
                nancy.cazorla@infomed.sld.cu
                consuelocorrea@infomed.sld.cu
                v_kouri@hotmail.com.cu
                yudira@infomed.sld.cu
                lissetteps@infomed.sld.cu
                lissette@ipk.sld.cu
                yudira@ipk.sld.cu
                mabel.aleman@infomed.sld.cu
                arlet@infomed.sld.cu
                celiama@ipk.sld.cu
                juan.marchena@infomed.sld.cu
                solar@infomed.sld.cu
                betsy@ipk.sld.cu
                clara@ipk.sld.cu
                hengge@hautzentrum-hengge.de
                Journal
                Springerplus
                Springerplus
                SpringerPlus
                Springer International Publishing (Cham )
                2193-1801
                16 May 2014
                16 May 2014
                2014
                : 3
                : 247
                Affiliations
                [ ]Sexually Transmitted Diseases Laboratory, Virology Department, Institute of Tropical Medicine “Pedro Kourí”, Havana City, Cuba
                [ ]Epidemiology and Statistic Department, Institute of Tropical Medicine “Pedro Kourí”, Havana City, Cuba
                [ ]University Pediatric Hospital “William Soler”, Havana City, Cuba
                [ ]University Pediatric Hospital of “Centro Habana”, Havana City, Cuba
                [ ]National Institute of Haematology and Immunology, Havana City, Cuba
                [ ]Respiratory Viruses Laboratory, Virology Department, Institute of Tropical Medicine “Pedro Kourí”, Havana City, Cuba
                [ ]Haut Zentrum (Skin Center), Duesseldorf, Germany
                [ ]Virology Department, Institute of Tropical Medicine ¨Pedro Kourí¨, Autopista Novia del Mediodia Km 6., La Lisa, Havana City, Cuba
                Article
                964
                10.1186/2193-1801-3-247
                4035497
                6f3d8fb7-c25d-4da7-a7f4-12b186d13cd2
                © Kourí et al.; licensee Springer. 2014

                This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.

                History
                : 16 March 2014
                : 7 May 2014
                Categories
                Research
                Custom metadata
                © The Author(s) 2014

                Uncategorized
                transplant,pediatric,cmv,cuba,viruses
                Uncategorized
                transplant, pediatric, cmv, cuba, viruses

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